FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity.
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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controlsCopy number variation at 1q21.1 associated with neuroblastomaPaired-end mapping reveals extensive structural variation in the human genomeMicroarray resources for genetic and genomic studies in chicken: a reviewFrom HLA-B27 to spondyloarthritis: a journey through the ER.Complex and multi-allelic copy number variation in human diseaseRecent advances in the genetics of autoimmune diseaseGenomic copy number variants: evidence for association with antibody response to anthrax vaccine adsorbedHigh basal activity of the PTPN22 gain-of-function variant blunts leukocyte responsiveness negatively affecting IL-10 production in ANCA vasculitisWegener's granulomatosis: a model of auto-antibodies in mucosal autoimmunityThe contribution of genetic variation and infection to the pathogenesis of ANCA-associated systemic vasculitisSimple and versatile molecular method of copy-number measurement using cloned competitorsComprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degenerationPsychomotor retardation with a 1q42.11–q42.12 deletionPopulation genomics of human gene expressionGenome-wide association study of copy number variations (CNVs) with opioid dependence.A genome-wide assessment of the role of untagged copy number variants in type 1 diabetes.Copy number variation in CNP267 region may be associated with hip bone size.Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease.A survey of copy-number variation detection tools based on high-throughput sequencing data.Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants.An Integrated Approach for RNA-seq Data NormalizationSeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data.Genome-Wide Association Study of Copy Number Variations in Patients with Familial Neurocardiogenic Syncope.Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.Tyrosine hydroxylase gene: another piece of the genetic puzzle of Parkinson's diseaseSmall deletion variants have stable breakpoints commonly associated with alu elements.Computing power and sample size for case-control association studies with copy number polymorphism: application of mixture-based likelihood ratio testContrasting genetic association of IL2RA with SLE and ANCA-associated vasculitisAssociation of FCGR3A and FCGR3B copy number variations with systemic lupus erythematosus and rheumatoid arthritis in Taiwanese patients.Personalized copy number and segmental duplication maps using next-generation sequencing.Quadruplex MAPH: improvement of throughput in high-resolution copy number screening.Copy number variation of FCGR genes in etiopathogenesis of sarcoidosisCopy number variants in genetic susceptibility and severity of systemic lupus erythematosusContribution of Human FcγRs to Disease with Evidence from Human Polymorphisms and Transgenic Animal StudiesFcgamma receptors: structure, function and role as genetic risk factors in SLEThe lupus family registry and repository.Genetic variation of the Fc gamma receptor 3B gene and association with rheumatoid arthritis.Genetic factors predisposing to systemic lupus erythematosus and lupus nephritis.Analysis of copy number variations among diverse cattle breeds.
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FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 21 May 2007
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
FCGR3B copy number variation i ...... organ-specific, autoimmunity.
@en
FCGR3B copy number variation i ...... organ-specific, autoimmunity.
@nl
type
label
FCGR3B copy number variation i ...... organ-specific, autoimmunity.
@en
FCGR3B copy number variation i ...... organ-specific, autoimmunity.
@nl
prefLabel
FCGR3B copy number variation i ...... organ-specific, autoimmunity.
@en
FCGR3B copy number variation i ...... organ-specific, autoimmunity.
@nl
P2093
P2860
P356
P1433
P1476
FCGR3B copy number variation i ...... organ-specific, autoimmunity.
@en
P2093
Adam de Smith
Alexandra I F Blakemore
Catherine J Owen
Charles D Pusey
Deborah S Cunninghame Graham
Enrico Petretto
H Terence Cook
Joanne M Heward
Lavanya Kamesh
Loic Guillevin
P2860
P2888
P304
P356
10.1038/NG2046
P407
P577
2007-05-21T00:00:00Z